A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677619



Internal ID9943724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142976779..142976937hg38UCSC Ensembl
chr8:144058196..144058354hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5809767, essv5402184, essv5601358, essv5617818, essv5656788, essv5913490, essv6500748, essv5765255, essv5672189, essv6484547, essv5800212, essv5414030, essv5798109, essv6188948
SamplesNA18924, NA11829, NA18504, NA20356, NA18510, NA19396, HG01350, NA07347, NA19138, HG01171, HG00701, NA18853, NA19401, NA19360
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677619
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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